نتائج البحث

1

Role of the KCNJ Gene Variants in the Clinical Outcome of Type 1 Diabetes

المؤلفون: Francesco Chiarelli, Concetta Di Giulio, Stefano Tumini, Liborio Stuppia, Valeria Castorani, Martina Provenzano, Lorena Matonti, Giovanni Prezioso, Daniela Iannucci, Laura Comegna, Annalisa Blasetti, Simone Franchini

المصدر: Hormone and Metabolic Research. 52:856-860

مصطلحات موضوعية: Blood Glucose, Male, 0301 basic medicine, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Type 2 diabetes, Bioinformatics, Biochemistry, Body Mass Index, Cohort Studies, 0302 clinical medicine, Endocrinology, Polymorphism (computer science), Genotype, Child, education.field_of_study, General Medicine, Prognosis, Female, Adult, medicine.medical_specialty, Adolescent, Population, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, 03 medical and health sciences, Insulin resistance, Internal medicine, Diabetes mellitus, medicine, Humans, Genetic Predisposition to Disease, Potassium Channels, Inwardly Rectifying, education, Genetic Association Studies, Glycated Hemoglobin, Type 1 diabetes, business.industry, Biochemistry (medical), medicine.disease, Diabetes Mellitus, Type 1, 030104 developmental biology, Case-Control Studies, Insulin Resistance, business, Biomarkers, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7733ca9fe72df079dd49d97d55f1604Test
https://doi.org/10.1055/a-1204-5443Test

2

Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients

المؤلفون: Erika Cecchin, Giuseppe Toffoli, Federico Innocenti, Alan Forrest, Deborah A. Nickerson, Amy S. Etheridge, Nancy J. Cox, Spinel Karas, Robert R. Bies, Karen L. Mohlke, Ron H.J. Mathijssen

المساهمون: Medical Oncology

المصدر: British Journal of Cancer, 126(4), 640-651. Nature Publishing Group
Br J Cancer

مصطلحات موضوعية: Oncology, Adult, Male, Cancer Research, medicine.medical_specialty, Bevacizumab, Pharmacogenomic Variants, Bilirubin, Population, Irinotecan, Polymorphism, Single Nucleotide, Article, chemistry.chemical_compound, Pharmacokinetics, SDG 3 - Good Health and Well-being, Internal medicine, Neoplasms, Genotype, Antineoplastic Combined Chemotherapy Protocols, medicine, Humans, Glucuronosyltransferase, education, Aged, Aged, 80 and over, education.field_of_study, Clinical Trials as Topic, biology, business.industry, Liver-Specific Organic Anion Transporter 1, Cancer, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, Middle Aged, medicine.disease, digestive system diseases, ErbB Receptors, chemistry, biology.protein, Administration, Intravenous, Female, business, SLCO1B1, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62ea219d07ad99d5cc228e98f7bdd0c6Test
https://pure.eur.nl/en/publications/3ab53839-bab3-4d00-bf51-f5c07b5d3416Test

3

Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes

المؤلفون: Dawit A. Yohannes, Katri Kaukinen, Katri Lindfors, Matti Nykter, Päivi Saavalainen, Aarno Palotie, Juliana X. M. Cerqueira, Kalle Kurppa, Lotta L. E. Koskinen, Elina Kilpeläinen, Anastasia Shcherban, Pilvi Laurikka, Heini Huhtala

المساهمون: Tampere University, BioMediTech, Department of Paediatrics, Clinical Medicine, Health Sciences, Department of Internal medicine, Immunomics, Department of Medical and Clinical Genetics, University of Helsinki, Research Programme of Molecular Medicine, Research Programs Unit, TRIMM - Translational Immunology Research Program, Genomics of Neurological and Neuropsychiatric Disorders, Institute for Molecular Medicine Finland, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, HUS Helsinki and Uusimaa Hospital District

المصدر: Journal of Human Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, Malabsorption, Genome-wide association study, VARIANTS, Genome-wide association studies, Coeliac disease, 0302 clinical medicine, MULTIPLE COMMON, Child, POPULATION, Genetics (clinical), Ataxin-2, RISK, education.field_of_study, Disease genetics, 1184 Genetics, developmental biology, physiology, Middle Aged, 3. Good health, Phenotype, Child, Preschool, 030211 gastroenterology & hepatology, Female, Genetic databases, Adult, Adolescent, Genotype, Population, Genetic predisposition to disease, Locus (genetics), Single-nucleotide polymorphism, 3121 Internal medicine, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Young Adult, Dermatitis herpetiformis, LINKAGE, Genetics, medicine, Diabetes Mellitus, Humans, GENOME-WIDE ASSOCIATION, education, Adaptor Proteins, Signal Transducing, Aged, Type 1 diabetes, business.industry, Infant, medicine.disease, Celiac Disease, 030104 developmental biology, Toll-Like Receptor 7, Toll-Like Receptor 8, Immunology, 3111 Biomedicine, business, Genome-Wide Association Study